Abstract:Key indicatorsSingle-crystal X-ray study T = 293 K Mean '(C±C) = 0.004 A Ê R factor = 0.026 wR factor = 0.072 Data-to-parameter ratio = 12.1 For details of how these key indicators were automatically derived from the article, see
“…There is only one kind of hydrogen bonds: N-H· · · Cl, which link the cations and anions to generate a two-dimensional supramolecular structure. All bond lengths and angles of the title compound are comparable with its analogues [5][6][7][8][9]. In detail, the bonding parameter of the title cations are in perfect accord with literature known 1Hbenzo[d] imidazol-3-ium salts [10,11].…”
Section: Commentsupporting
confidence: 84%
“…Known as organic bases, benzimidazole and their derivatives are readily to be protonated. There are some records of 1or 2-substituted benzimidazoles used as cations to counter the negative charges of tetrachloridozincate anions [5][6][7][8][9]. As shown in the figure, the asymmetric unit consists of two 2propyl-1H-benzimidazol-3-ium cations and one tetrachloridozincate anion.…”
“…There is only one kind of hydrogen bonds: N-H· · · Cl, which link the cations and anions to generate a two-dimensional supramolecular structure. All bond lengths and angles of the title compound are comparable with its analogues [5][6][7][8][9]. In detail, the bonding parameter of the title cations are in perfect accord with literature known 1Hbenzo[d] imidazol-3-ium salts [10,11].…”
Section: Commentsupporting
confidence: 84%
“…Known as organic bases, benzimidazole and their derivatives are readily to be protonated. There are some records of 1or 2-substituted benzimidazoles used as cations to counter the negative charges of tetrachloridozincate anions [5][6][7][8][9]. As shown in the figure, the asymmetric unit consists of two 2propyl-1H-benzimidazol-3-ium cations and one tetrachloridozincate anion.…”
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